A controlled-release strategy for the generation of cross-linked hydrogel microstructures

被引:96
作者
Franzesi, Giovanni Talei
Ni, Bin
Ling, Yibo
Khademhosseini, Ali [1 ]
机构
[1] Harvard Univ, MIT, Div Hlth Sci & Technol, Cambridge, MA 02138 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Biomed Engn,Dept Med, Cambridge, MA 02139 USA
关键词
D O I
10.1021/ja065867x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Microscale hydrogels of controlled sizes and shapes are useful for cell-based screening, in vitro diagnostics, tissue engineering, and drug delivery. However, the rapid cross-linking of many chemically and pH cross-linkable hydrogel materials prevents the application of existing micromolding techniques. In this work we present a method for fabricating micromolded calcium alginate and chitosan structures through controlled release of the gelling agent from a hydrogel mold. Replica molding was employed to generate patterned membranes, whereas microtransfer molding was used to produce microparticles of controlled shapes. To explore the viability of this technique for producing complex tissue engineering micro-architectures, this approach was used to generate cell-laden size- and shape-controlled 3D microgels as well as composite hydrogels with well-defined spatially segregated regions. In addition, shape-controlled microstructures that can exhibit differential release properties were loaded with macromolecules to verify the potential of this approach for drug delivery applications. Copyright © 2006 American Chemical Society.
引用
收藏
页码:15064 / 15065
页数:2
相关论文
共 16 条
[1]   A microfluidic biomaterial [J].
Cabodi, M ;
Choi, NW ;
Gleghorn, JP ;
Lee, CSD ;
Bonassar, LJ ;
Stroock, AD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (40) :13788-13789
[2]   Large porous particles for pulmonary drug delivery [J].
Edwards, DA ;
Hanes, J ;
Caponetti, G ;
Hrkach, J ;
BenJebria, A ;
Eskew, ML ;
Mintzes, J ;
Deaver, D ;
Lotan, N ;
Langer, R .
SCIENCE, 1997, 276 (5320) :1868-1871
[3]   Hydrogels for biomedical applications [J].
Hoffman, Allan S. .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 :18-23
[4]   Continuous fabrication of biocatalyst immobilized microparticles using photopolymerization and immiscible liquids in microfluidic systems [J].
Jeong, WJ ;
Kim, JY ;
Choo, J ;
Lee, EK ;
Han, CS ;
Beebe, DJ ;
Seong, GH ;
Lee, SH .
LANGMUIR, 2005, 21 (09) :3738-3741
[5]   Conformal coating of mammalian cells immobilized onto magnetically driven beads [J].
Khademhosseini, A ;
May, MH ;
Sefton, MV .
TISSUE ENGINEERING, 2005, 11 (11-12) :1797-1806
[6]   Calcium alginate microspheres of Bacillus subtilis [J].
Lamas, MC ;
Bregni, C ;
D'Aquino, M ;
Degrossi, J ;
Firenstein, R .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2001, 27 (08) :825-829
[7]   Advances in biomaterials, drug delivery, and bionanotechnology [J].
Langer, R ;
Peppas, NA .
AICHE JOURNAL, 2003, 49 (12) :2990-3006
[8]   TISSUE ENGINEERING [J].
LANGER, R ;
VACANTI, JP .
SCIENCE, 1993, 260 (5110) :920-926
[9]   Three-dimensional photopatterning of hydrogels containing living cells [J].
Liu, VA ;
Bhatia, SN .
BIOMEDICAL MICRODEVICES, 2002, 4 (04) :257-266
[10]   Vascularized organoid engineered by modular assembly enables blood perfusion [J].
McGuigan, Alison P. ;
Sefton, Michael V. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (31) :11461-11466